Consensus treatment plans for new‐onset systemic juvenile idiopathic arthritis

EM Dewitt, Y Kimura, T Beukelman… - Arthritis care & …, 2012 - Wiley Online Library
EM Dewitt, Y Kimura, T Beukelman, PA Nigrovic, K Onel, S Prahalad, R Schneider, ML Stoll…
Arthritis care & research, 2012Wiley Online Library
Objective There is wide variation in therapeutic approaches to systemic juvenile idiopathic
arthritis (JIA) among North American rheumatologists. Understanding the comparative
effectiveness of the diverse therapeutic options available for treatment of systemic JIA can
result in better health outcomes. The Childhood Arthritis and Rheumatology Research
Alliance (CARRA) developed consensus treatment plans and standardized assessment
schedules for use in clinical practice to facilitate such studies. Methods Case‐based surveys …
Objective
There is wide variation in therapeutic approaches to systemic juvenile idiopathic arthritis (JIA) among North American rheumatologists. Understanding the comparative effectiveness of the diverse therapeutic options available for treatment of systemic JIA can result in better health outcomes. The Childhood Arthritis and Rheumatology Research Alliance (CARRA) developed consensus treatment plans and standardized assessment schedules for use in clinical practice to facilitate such studies.
Methods
Case‐based surveys were administered to CARRA members to identify prevailing treatments for new‐onset systemic JIA. A 2‐day consensus conference in April 2010 employed modified nominal group technique to formulate preliminary treatment plans and determine important data elements for collection. Followup surveys were employed to refine the plans and assess clinical acceptability.
Results
The initial case‐based survey identified significant variability among current treatment approaches for new‐onset systemic JIA, underscoring the utility of standardized plans to evaluate comparative effectiveness. We developed 4 consensus treatment plans for the first 9 months of therapy, as well as case definitions and clinical and laboratory monitoring schedules. The 4 treatment regimens included glucocorticoids only, or therapy with methotrexate, anakinra, or tocilizumab, with or without glucocorticoids. This approach was approved by >78% of the CARRA membership.
Conclusion
Four standardized treatment plans were developed for new‐onset systemic JIA. Coupled with data collection at defined intervals, use of these treatment plans will create the opportunity to evaluate comparative effectiveness in an observational setting to optimize initial management of systemic JIA.
Wiley Online Library